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IL-21 Receptor Expression in Human Tendinopathy
被引:23
|作者:
Campbell, Abigail L.
[1
,2
]
Smith, Nicola C.
[1
]
Reilly, James H.
[1
]
Kerr, Shauna C.
[1
]
Leach, William J.
[3
]
Fazzi, Umberto G.
[3
]
Rooney, Brian P.
[3
]
Murrell, George A. C.
[4
]
Millar, Neal L.
[1
,3
]
机构:
[1] Vet & Life Sci Univ Glasgow, Inst Infect Immun & Inflammat, Coll Med, Glasgow G12 8TA, Lanark, Scotland
[2] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[3] Univ Glasgow, Western Infirm, Dept Orthopaed Surg, Glasgow G11 6NT, Lanark, Scotland
[4] Univ New S Wales, Dept Orthopaed Surg, Orthopaed Res Inst, Sydney, NSW, Australia
基金:
英国惠康基金;
关键词:
INTERLEUKIN-21;
RECEPTOR;
FLEXOR TENDON;
PATHOGENESIS;
FIBROBLASTS;
CYTOKINES;
INFLAMMATION;
IL-1-BETA;
APOPTOSIS;
VARIANTS;
RAT;
D O I:
10.1155/2014/481206
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The pathogenetic mechanisms underlying tendinopathy remain unclear, with much debate as to whether inflammation or degradation has the prominent role. Increasing evidence points toward an early inflammatory infiltrate and associated inflammatory cytokine production in human and animal models of tendon disease. The IL-21/IL-21R axis is a proinflammatory cytokine complex that has been associated with chronic inflammatory diseases including rheumatoid arthritis and inflammatory bowel disease. This project aimed to investigate the role and expression of the cytokine/receptor pair IL-21/IL-21R in human tendinopathy. We found significantly elevated expression of IL-21 receptormessage and protein in human tendon samples but found no convincing evidence of the presence of IL-21 at message or protein level. The level of expression of IL-21R message/protein in human tenocytes was significantly upregulated by proinflammatory cytokines (TNF alpha/IL-1 beta) in vitro. These findings demonstrate that IL-21R is present in early human tendinopathy mainly expressed by tenocytes and macrophages. Despite a lack of IL-21 expression, these data again suggest that early tendinopathy has an inflammatory/cytokine phenotype, which may provide novel translational targets in the treatment of tendinopathy.
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